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Ammonium Chloride → 7-[(Ethylsulfanyl)methyl]-1H-indole

HRID 561374
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HRID 561374 반응식
[CH2:1]([S:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[N+:11]([O-])=O)[CH3:2].[CH:14]([Mg]Br)=[CH2:15].[Cl-].[NH4+]>O1CCCC1>[CH2:1]([S:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:6]=1[NH:11][CH:15]=[CH:14]2)[CH3:2]
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참가 물질

5

반응물 3

HCID 25517Ammonium ChlorideHCID 583923871-[(Ethylsulfanyl)methyl]-2-nitrobenzeneHCID 178418507HCID 178418507, 화합물

생성물 1

HCID 583922897-[(Ethylsulfanyl)methyl]-1H-indole

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

반응 조건

온도
-78 °C

실험 절차

A solution of 7.40 g (37.5 mmol) of the compound from Example 3A in 195 ml of tetrahydrofuran was added dropwise to 134 ml (93.8 mmol) of a 0.7N solution of vinylmagnesium bromide in tetrahydrofuran under argon at −78° C., and the mixture was stirred at −78° C. for 2 h. The reaction mixture was then slowly added to an ice-cold, saturated aqueous ammonium chloride solution and extracted three times with ethyl acetate. The combined organic phases were washed with saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and concentrated. The residue was purified by flash chromatography (mobile phase: cyclohexane/ethyl acetate 9/1) to result in 4.98 g (69% of theory) of the title compound.

후처리

  1. extractionextracted three times with ethyl acetate
  2. washThe combined organic phases were washed with saturated aqueous sodium chloride solution
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe residue was purified by flash chromatography (mobile phase: cyclohexane/ethyl acetate 9/1)

출처 및 근거

ORD 기록
ord-460421825b1847768d3b1c2428fae6ea
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08063234B2

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